Study identifier:4522IL/0032
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
An 18-week, randomised, double-blind, multicentre, placebo-controlled trial to evaluate the efficacy and safety of rosuvastatin (5 and 10 mg) in the treatment of hypercholesterolaemic postmenopausal women receiving hormone replacement therapy
dyslipidaemia
Phase 3
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Interventional
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Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2013 by AstraZeneca
AstraZeneca
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No locations available
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